2-bromo-1-chloro-4-(trifluoromethoxy)benzene
98%
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This chemical is primarily used in the synthesis of more complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring bromo, chloro, and trifluoromethoxy substituents, makes it a valuable intermediate for constructing molecules with specific electronic and steric properties. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active compounds. Additionally, its trifluoromethoxy group is of interest in medicinal chemistry due to its ability to enhance the metabolic stability and lipophilicity of drug candidates. In agrochemicals, it can be utilized to develop pesticides or herbicides with improved efficacy. Its halogenated structure also makes it a candidate for materials science applications, such as in the development of liquid crystals or organic electronics.
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